ClinicalTrials.gov record
Completed Phase 2 Interventional Results available

Safety Study to Assess IV Zanamivir for Treatment of Influenza Infection in Patients Who Are in Hospital

ClinicalTrials.gov ID: NCT01014988

Public ClinicalTrials.gov record NCT01014988. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 20, 2026, 8:47 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

An Open-label, Multi-center, Single Arm Study to Evaluate the Safety and Tolerability of Intravenous Zanamivir in the Treatment of Hospitalized Adult, Adolescent and Pediatric Subjects With Confirmed Influenza Infection

Study identification

NCT ID
NCT01014988
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
202 participants

Conditions and interventions

Interventions

  • zanamivir aqueous solution Drug

Drug

Eligibility (public fields only)

Age range
6 Months and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 31, 2009
Primary completion
Jan 31, 2015
Completion
Jan 31, 2015
Last update posted
Mar 27, 2017

2009 – 2015

United States locations

U.S. sites
40
U.S. states
27
U.S. cities
36
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35233
GSK Investigational Site Phoenix Arizona 85023
GSK Investigational Site Little Rock Arkansas 72202
GSK Investigational Site San Diego California 92123
GSK Investigational Site Stamford Connecticut 06902
GSK Investigational Site Washington D.C. District of Columbia 20007
GSK Investigational Site Washington D.C. District of Columbia 20010
GSK Investigational Site Gainesville Florida 32608
GSK Investigational Site Tampa Florida 33606
GSK Investigational Site Atlanta Georgia 30322
GSK Investigational Site Decatur Georgia 30033
GSK Investigational Site Indianapolis Indiana 46202
GSK Investigational Site Topeka Kansas 66604
GSK Investigational Site Louisville Kentucky 40202
GSK Investigational Site New Orleans Louisiana 70112
GSK Investigational Site Boston Massachusetts 02115-5724
GSK Investigational Site Boston Massachusetts 02115
GSK Investigational Site Saint Paul Minnesota 55102
GSK Investigational Site Kansas City Missouri 64108
GSK Investigational Site St Louis Missouri 63110
GSK Investigational Site Butte Montana 59701
GSK Investigational Site Camden New Jersey 08103
GSK Investigational Site New Hyde Park New York 11040
GSK Investigational Site Chapel Hill North Carolina 27514
GSK Investigational Site Charlotte North Carolina 28203
GSK Investigational Site Cleveland Ohio 44106
GSK Investigational Site Columbus Ohio 43205
GSK Investigational Site Toledo Ohio 43606
GSK Investigational Site Portland Oregon 97239
GSK Investigational Site Philadelphia Pennsylvania 19102
GSK Investigational Site Pittsburgh Pennsylvania 15224
GSK Investigational Site Memphis Tennessee 38103
GSK Investigational Site Memphis Tennessee 38105
GSK Investigational Site Dallas Texas 75231
GSK Investigational Site Dallas Texas 75235
GSK Investigational Site Fort Worth Texas 76104
GSK Investigational Site Houston Texas 77030
GSK Investigational Site Salt Lake City Utah 84113
GSK Investigational Site Richmond Virginia 23249
GSK Investigational Site Milwaukee Wisconsin 53201

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 70 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01014988, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 27, 2017 · Synced May 20, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01014988 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →